The use of water fragrant edge extract to reduce skin inflammation caused by keratinocytes exposed to ultraviolet light and promote skin keratin metabolism
A technology of skin cutin and cutin cells, applied in skin care preparations, skin diseases, drug combinations, etc., can solve problems such as sensitive water retention capacity, skin fragility, and thickened cuticle
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Embodiment 1
[0020] Embodiment 1 The preparation method of the water fragrant edge extract of the present invention
[0021] Cyperusrotundus (Cyperusrotundus) is a plant of Cyperaceae, also known as Cyperus officinalis, fragrant head grass, earth incense, stinky head incense, etc., water fragrant edge is known to have the effects of relieving pain, regulating menstruation, dispelling cold hernia and relieving abdominal pain. .
[0022] In one embodiment of the present invention, the whole plant of S. serrata is washed, and the extraction solvent of the whole plant of S. serrata after washing and water, alcohol, or mixture of alcohol and water is taken at a liquid-solid ratio of 5-20: 1-5 Mix and homogenize, and perform extraction at 50-100°C, preferably 75°C-95°C, for 0.5-3 hours to obtain a crude extract. After extraction, it was cooled to room temperature, and the crude extract was filtered through a 400-mesh sieve to obtain a filtrate. Finally, the filtrate is concentrated under reduc...
Embodiment 2
[0023] Example 2 The effect of the water fragrant edge extract of the present invention on promoting the proliferation of skin keratinocytes
[0024] The invention uses human primary epidermal keratinocytes (human primary epidermal keratinocytes, HPEKp) to carry out the experiment of skin keratinocyte proliferation. The human primary skin keratinocytes were purchased from CELLnTEC (Switzerland) under the number HPEK-50. The cells were cultured in serum-free keratinocyte-SFM (Gibco, USA, No. #10724-011).
[0025] The analysis was performed using the Cell Proliferation Reagent Kit (purchased from Roche, Switzerland, no. 11647229001). First, in a 96-well culture dish, each well was seeded with 3 × 10 3 Individual human primary skin keratinocytes were cultured with the above-mentioned culture medium at 37°C for 2 hours, and 100 μl of blank control group (mock) or 1.25 mg / mL of the extract of the present invention, and 10 μl of 100 μM brominated deoxygenation were added to each w...
Embodiment 3
[0027] Example 3 The water-flavor extract of the present invention inhibits the secretion of interleukin-8 (IL-8) due to ultraviolet irradiation
[0028] Since it is known that interleukin-8 (IL-8) is a cytokine and has the function of promoting the production of inflammatory response, the present invention further detects the ability of the Shuixiangleng extract to inhibit the secretion of interleukin-8, This secretion is caused by exposure of keratinocytes to ultraviolet light. First, in a 24-well culture dish, add 500 μl of the above culture medium to each well and implant 5×10 4 keratinocytes were cultured at 37°C for 24 hours. The culture medium was removed without disturbing the attached cells, and the keratinocytes were divided into four groups (n=3), respectively (1) the blank control group (mock) added culture medium and did not irradiate UVB, (2) positive In the control group, keratinocytes were added to the culture medium and incubated at 37°C for 2 hours and then...
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